Piperidine → HCID 59829629, compound

HRID 602486Notes

Reaction equation

HRID 602486 reaction equation
C(OC([N:8]1[CH2:12][C@@H:11]([NH:13][C:14]([C:16]2[C:24]3[C:19](=[CH:20][CH:21]=[CH:22][CH:23]=3)[N:18]([CH:25]([CH3:27])[CH3:26])[N:17]=2)=[O:15])[CH2:10][C@H:9]1[CH2:28][C:29](O)=[O:30])=O)(C)(C)C.[NH:32]1[CH2:37][CH2:36][CH2:35][CH2:34][CH2:33]1>>[CH:25]([N:18]1[C:19]2[C:24](=[CH:23][CH:22]=[CH:21][CH:20]=2)[C:16]([C:14]([NH:13][C@H:11]2[CH2:10][C@@H:9]([CH2:28][C:29](=[O:30])[N:32]3[CH2:37][CH2:36][CH2:35][CH2:34][CH2:33]3)[NH:8][CH2:12]2)=[O:15])=[N:17]1)([CH3:27])[CH3:26]

Participants

3

Procedure

The title compound was prepared according to the procedure described in step 1 of Example 7 from ((2S,4S)-1-(tert-butoxycarbonyl)-4-{[(1-isopropyl-1H-indazol-3-yl)carbonyl]amino}pyrrolidin-2-yl)acetic acid (step 1 of Example 13) and piperidine.

Sources & evidence

ORD record
ord-5c1854462faf4c3faf4c11322f69995a
Source dataset
uspto-grants-2011_03
Patent number
US07906532B2

Reaction notes

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