HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1018693Generated: October 30, 2026
Diisopropylethylamine → HCID 54404418, compound
https://huagongshe.com/reaction/1018693
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Reactant | HCID 131723645 | HCID 131723645 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 54404418 | HCID 54404418 | 173.5% |
Reaction Steps
To a solution of (1S-trans)-[3-(Phenylmethoxy)carbonyl]-1,2,2-trimethylcyclopentane-1-carboxylic acid, 36-F-1, (503.7 mg) in DMF(5 mL) and DIEA(3 mL) was added O-(7-Azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate(731.7 mg) and the reaction stirred at ambient temperature for 1 hour. To the reaction was added 4-[(2,6-dichlorobenzoyl)amino]-D-phenylalanine methyl ester, hydrochloride salt(698.6 mg), 37-B-2, and the reaction stirred for 5 days. The reaction was then diluted with water and extracted with AcOEt. The concentrated extract was purified by flash chromatography on silica gel eluting with methanol in methylene chloride to obtain (1S-trans)-N-[(3-(Phenylmethoxy)carbonyl)-1,2,2-trimethylcyclopentyl)carbonyl]-4-[(2,6-dichlorobenzoyl)amino]-D-phenylalanine methyl ester(1.1024 g). Physical properties as follows: 1H NMR (CDCl3) δ7.82 (1 H), 7.58 (2 H), 7.28 (8 H), 7.05 (2 H), 6.07 (1 H), 5.06 (2 H), 4.74 (1 H), 3.66 (3 H), 3.07 (3 H), 2.05 (3 H), 1.53 (1 H), 1.21 (3 H), 0.90 (3 H), 0.75 (3 H); MS−ESI (m/z): 637([M−H−]); MS−ESI (m/z): 661([M+Na]+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06482849B1 |
|---|
| Source dataset | uspto-grants-2002_11 |
|---|
| ORD ID | ord-d79665d4654a47dfa8fa373ca07d171d |
|---|
| Source note | uspto-grants-2002_11 |
|---|