HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2069467Generated: October 31, 2026
N,O-Dimethylhydroxylamine → 2-Isopropylamino-6-methyl-pyrimidine-4-carboxylic acid methoxy-methyl-amide
https://huagongshe.com/reaction/2069467
Participants
| Role | Name | HCID | Charge |
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| Reactant | N,O-Dimethylhydroxylamine | HCID 14232 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate | HCID 2733207 | — |
| Reactant | 2-(Isopropylamino)-6-methylpyrimidine-4-carboxylic acid | HCID 66933715 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Isopropylamino-6-methyl-pyrimidine-4-carboxylic acid methoxy-methyl-amide | HCID 86645311 | 98.3% |
Reaction Steps
To a solution of 2-isopropylamino-6-methyl-pyrimidine-4-carboxylic acid (2.0 g, 10.2 mmol) in DCM (45 mL), DIPEA (8.8 mL, 51.2 mmol) followed by TBTU (3.9 g, 12.3 mmol) is added. The mixture is stirred at rt for 30 min before N,O-dimethylhydroxylamine (1.20 g, 12.3 mmol) is added. The mixture is stirred at rt for 18 h before it is diluted with DCM, washed with sat. aq. NaHCO3, followed by water, dried over MgSO4, filtered and concentrated. The crude product is purified by CC on silica gel eluting with heptane:EA 1:2 to give 2-isopropylamino-6-methyl-pyrimidine-4-carboxylic acid methoxy-methyl-amide (2.39 g) as a yellow oil; LC-MS: tR=0.66 min, [M+H]+=239.03; 1H NMR (D6-DMSO): δ 1.14 (d, J=6.5 Hz, 6H), 2.28 (s, 3H), 3.23 (s, 3H), 3.67 (s, 3H), 4.05 (m, 1H), 6.50 (s br, 1H), 7.12 (s br, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08299086B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-026240c4ae69424b99e69041d31afc53 |
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| Source note | uspto-grants-2012_10 |
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