Sodium Hydroxide → HCID 52938191, compound

HRID 1400123Notes

Reaction equation

HRID 1400123 reaction equation
[NH2:1][C:2]1[N:11]=[C:10]([C:12]([N:14]2[CH2:22][C:21]3[C:16](=[CH:17][CH:18]=[CH:19][CH:20]=3)[CH2:15]2)=[O:13])[C:9]2[C:4](=[CH:5][CH:6]=[C:7]([CH2:23][C:24]([O:26]CC)=[O:25])[CH:8]=2)[N:3]=1.[OH-].[Na+]>O1CCCC1>[NH2:1][C:2]1[N:11]=[C:10]([C:12]([N:14]2[CH2:15][C:16]3[C:21](=[CH:20][CH:19]=[CH:18][CH:17]=3)[CH2:22]2)=[O:13])[C:9]2[C:4](=[CH:5][CH:6]=[C:7]([CH2:23][C:24]([OH:26])=[O:25])[CH:8]=2)[N:3]=1

Participants

4

Conditions

Temperature
23 °C

Procedure

2.7 g of ethyl 2-[2-amino-4-(isoindoline-2-carbonyl)quinazolin-6-yl]acetate are dissolved in 40 ml of tetrahydrofuran, and 25 ml of 2N sodium hydroxide solution are added. The mixture is stirred at 23° C. for 12 h, evaporated to dryness in vacuo, taken up in 10 ml of water and adjusted to pH 2 using 7 ml of 25% hydrochloric acid. The resultant precipitate is filtered off and dried in vacuo.

Workup

  1. customevaporated to dryness in vacuo
  2. filtrationThe resultant precipitate is filtered off
  3. customdried in vacuo

Sources & evidence

ORD record
ord-6622c317bd8544f69e57e24a6276ce61
Source dataset
uspto-grants-2014_12
Patent number
US08906930B2

Reaction notes

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