HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(2,3-dihydroxypropoxy)-3,4-difluoro-2-(2-fluoro-4-iodoanilino)benzamide → 5-Chloro-2-(2-chloro-4-iodo-phenylamino)-N-[(R)-2,3-dihydroxy-propoxy]-3,4-difluoro-benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(2,3-dihydroxypropoxy)-3,4-difluoro-2-(2-fluoro-4-iodoanilino)benzamide | HCID 10206158 | — |
| Reactant | (R)-O-((2,2-Dimethyl-1,3-dioxolan-4-yl)methyl)hydroxylamine | HCID 11298047 | — |
| Reactant | 2-(2-Chloro4-iodophenylamino)-5-chloro-3,4-difluorobenzoic acid | HCID 22285923 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-Chloro-2-(2-chloro-4-iodo-phenylamino)-N-[(R)-2,3-dihydroxy-propoxy]-3,4-difluoro-benzamide | HCID 10128679 | — |
Reaction Steps
Prepared from (R)-O-(2,2-dimethyl-[1,3]dioxolan-4-ylmethyl)-hydroxylamine and 5-chloro-2-(2-chloro-4-iodo-phenylamino)-3,4-difluoro-benzoic acid by the procedure described for N-(2,3-dihydroxy-propoxy)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-benzamide: m.p. 155-156° C.; [α]=−5.1° (c=3.5 mg/mL, ethanol); 1NMR (400 MHz, DMSO-d6) δ 12.03 (s, 1), 8.83 (s, 1H), 7.76 (s, 1H), 7.66 (d, 1H, J=6.8 Hz), 7.47 (d, 1H, J=8.5 Hz), 6.68 (t, 1H, J=6.6 Hz), 4.83 (bs, 1H), 4.60 (bs, 1H), 3.89-3.92 (m, 1H), 3.68-3.76 (m, 2H), 3.30 (2H, partially hidden by HDO); MS (APCI+)=533.0/535.0; Anal.calcd/found for C16H13Cl2F2IN2O4: C, 36.05/36.04; H, 2.46/2.25; N, 5.25/5.10; F, 7.13/7.18; Cl, 13.30, 13.50; I, 23.80, 24.02.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06960614B2 |
| Source dataset | uspto-grants-2005_11 |
| ORD ID | ord-b0f8e33037b14ddea1d43e7a6d4722d3 |
| Source note | uspto-grants-2005_11 |